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Endophilin A1 Promotes Actin Polymerization in Dendritic Spines Required for Synaptic Potentiation
Endophilin A1 is a member of the N-BAR domain-containing endophilin A protein family that is involved in membrane dynamics and trafficking. At the presynaptic terminal, endophilin As participate in synaptic vesicle recycling and autophagosome formation. By gene knockout studies, here we report that...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985315/ https://www.ncbi.nlm.nih.gov/pubmed/29892212 http://dx.doi.org/10.3389/fnmol.2018.00177 |
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author | Yang, Yanrui Chen, Jiang Guo, Zhenzhen Deng, Shikun Du, Xiangyang Zhu, Shaoxia Ye, Chang Shi, Yun S. Liu, Jia-Jia |
author_facet | Yang, Yanrui Chen, Jiang Guo, Zhenzhen Deng, Shikun Du, Xiangyang Zhu, Shaoxia Ye, Chang Shi, Yun S. Liu, Jia-Jia |
author_sort | Yang, Yanrui |
collection | PubMed |
description | Endophilin A1 is a member of the N-BAR domain-containing endophilin A protein family that is involved in membrane dynamics and trafficking. At the presynaptic terminal, endophilin As participate in synaptic vesicle recycling and autophagosome formation. By gene knockout studies, here we report that postsynaptic endophilin A1 functions in synaptic plasticity. Ablation of endophilin A1 in the hippocampal CA1 region of mature mouse brain impairs long-term spatial and contextual fear memory. Its loss in CA1 neurons postsynaptic of the Schaffer collateral pathway causes impairment in their AMPA-type glutamate receptor-mediated synaptic transmission and long-term potentiation. In KO neurons, defects in the structural and functional plasticity of dendritic spines can be rescued by overexpression of endophilin A1 but not A2 or A3. Further, endophilin A1 promotes actin polymerization in dendritic spines during synaptic potentiation. These findings reveal a physiological role of endophilin A1 distinct from that of other endophilin As at the postsynaptic site. |
format | Online Article Text |
id | pubmed-5985315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59853152018-06-11 Endophilin A1 Promotes Actin Polymerization in Dendritic Spines Required for Synaptic Potentiation Yang, Yanrui Chen, Jiang Guo, Zhenzhen Deng, Shikun Du, Xiangyang Zhu, Shaoxia Ye, Chang Shi, Yun S. Liu, Jia-Jia Front Mol Neurosci Neuroscience Endophilin A1 is a member of the N-BAR domain-containing endophilin A protein family that is involved in membrane dynamics and trafficking. At the presynaptic terminal, endophilin As participate in synaptic vesicle recycling and autophagosome formation. By gene knockout studies, here we report that postsynaptic endophilin A1 functions in synaptic plasticity. Ablation of endophilin A1 in the hippocampal CA1 region of mature mouse brain impairs long-term spatial and contextual fear memory. Its loss in CA1 neurons postsynaptic of the Schaffer collateral pathway causes impairment in their AMPA-type glutamate receptor-mediated synaptic transmission and long-term potentiation. In KO neurons, defects in the structural and functional plasticity of dendritic spines can be rescued by overexpression of endophilin A1 but not A2 or A3. Further, endophilin A1 promotes actin polymerization in dendritic spines during synaptic potentiation. These findings reveal a physiological role of endophilin A1 distinct from that of other endophilin As at the postsynaptic site. Frontiers Media S.A. 2018-05-28 /pmc/articles/PMC5985315/ /pubmed/29892212 http://dx.doi.org/10.3389/fnmol.2018.00177 Text en Copyright © 2018 Yang, Chen, Guo, Deng, Du, Zhu, Ye, Shi and Liu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Yang, Yanrui Chen, Jiang Guo, Zhenzhen Deng, Shikun Du, Xiangyang Zhu, Shaoxia Ye, Chang Shi, Yun S. Liu, Jia-Jia Endophilin A1 Promotes Actin Polymerization in Dendritic Spines Required for Synaptic Potentiation |
title | Endophilin A1 Promotes Actin Polymerization in Dendritic Spines Required for Synaptic Potentiation |
title_full | Endophilin A1 Promotes Actin Polymerization in Dendritic Spines Required for Synaptic Potentiation |
title_fullStr | Endophilin A1 Promotes Actin Polymerization in Dendritic Spines Required for Synaptic Potentiation |
title_full_unstemmed | Endophilin A1 Promotes Actin Polymerization in Dendritic Spines Required for Synaptic Potentiation |
title_short | Endophilin A1 Promotes Actin Polymerization in Dendritic Spines Required for Synaptic Potentiation |
title_sort | endophilin a1 promotes actin polymerization in dendritic spines required for synaptic potentiation |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985315/ https://www.ncbi.nlm.nih.gov/pubmed/29892212 http://dx.doi.org/10.3389/fnmol.2018.00177 |
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